This course provides a comprehensive overview of monitoring activities conducted during clinical trials to ensure compliance with regulatory requirements and Good Clinical Practice (GCP). It covers key monitoring processes including routine site monitoring, CRF review and source data verification, drug accountability, safety reporting and pharmacovigilance, and study site close-out.

Learners will understand the roles and responsibilities of monitors, investigators, sponsors, and site staff in maintaining data quality and subject safety. The course also explains documentation practices, issue resolution, and regulatory expectations throughout the monitoring lifecycle.

By the end of the module, participants will gain practical knowledge of how clinical trials are supervised to ensure accuracy, integrity, and regulatory compliance.

Indian students: Choose the Offline Payment option at Checkout. Once your Order is created you will receive an email with a link to complete your payment of INR 19,999.